Taiwan FDA registration 7bb960a6926719416124cd7f72e2bb8b
Vitex Biochemical Products Therapeutic Quality Assurance Fluids I, II and III
TW: 維特司生化產品治療性藥物監控品質確認液 I,II 和 III
Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Sep 14, 2005 – Sep 14, 2025ExpiredRegistration details
- Analysis ID
- 7bb960a6926719416124cd7f72e2bb8b
- Customs Code
- DHA00601236006
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Vetex Biochemical Products Therapeutic Substance Monitoring Quality Confirmation Solution is used to monitor the performance of Vitex Biochemical Systems.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 2005
- Expiry Date
- Sep 14, 2025
About this record
Access comprehensive regulatory information for Vitex Biochemical Products Therapeutic Quality Assurance Fluids I, II and III in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7bb960a6926719416124cd7f72e2bb8b and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices